| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001206673.1 | 322 | Missense Mutation | ATT,GTT | I103V | NP_001193602.1 |
| NM_181533.3 | 322 | UTR 5 | NP_853511.2 | ||
| NM_181814.1 | 322 | Intron | NP_861535.1 | ||
| XM_006720052.1 | 322 | Intron | XP_006720115.1 | ||
| XM_011536472.1 | 322 | Missense Mutation | ATT,GTT | I103V | XP_011534774.1 |
| XM_011536474.2 | 322 | Missense Mutation | ATT,GTT | I61V | XP_011534776.1 |
| XM_017021031.1 | 322 | UTR 5 | XP_016876520.1 |